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“The Ca2+-induced Ca2+ release blocker tetracaine inhibited the rise in [Ca2+]i induced by both caffeine and ATP, with apparent inhibitory constants of 70 μM and 100 μM, respectively.”
American journal of respiratory and critical care medicine • 2000 | View Paper
“While tetracaine inhibits sperm motility and caffeine has an excitatory action, the combination of these two substances balance the effects, producing a motility quite similar to that of control cells.”
“ Caffeine (10 mM) produced large transient currents that reversed close to the Cl(-) equilibrium potential and were blocked by 1 mM DIDS or 100 microM tetracaine.”
Investigative ophthalmology & visual science • 2009 | View Paper
“Increase in Ca2+-signals with fluo 4 and rhod-2 caused by caffeine were reduced by tetracaine and oligomycin plus carbonyl cyanide m-chlorophenylhydrazone, respectively.”
“The release of ATP induced by caffeine (3 mM) was almost completely inhibited by ryanodine and tetracaine , but not by 2-APB, thus being mediated by ryanodine receptors (RyR).”
Naunyn-Schmiedeberg's Archives of Pharmacology • 2008 | View Paper
“The channel activator, caffeine , and the CRC inhibitor, tetracaine , are shown to interact competitively, which suggests that there exists a common site(s) on the CRC, that integrates the donor/acceptor effects of ligands.”
Antioxidants & redox signaling • 2007 | View Paper
“ Caffeine at 0.5 mM in the presence of the same concentration of tetracaine failed to potentiate release flux independently of the test voltage applied.”
Journal of Muscle Research & Cell Motility • 2006 | View Paper
“Lower concentrations of tetracaine (0.5mm) and procaine (⩽10mm) blocked contractions due to caffeine (at pCa ⩾6.73), sulphydryl oxidizing agents, or Ca2+-induced Ca2+ release (CICR).”
Journal of Muscle Research & Cell Motility • 2005 | View Paper
“ Caffeine also antagonized the actions of tetracaine on the total available qgamma charge, but did so only at the low and not at the high applied concentrations.”